Clinical Profile and Health Disparities in a Multiethnic Cohort of Patients With Hypertrophic Cardiomyopathy.
Full text not available from this repository.Item Type: | Article |
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Status: | Published |
Official URL: | https://doi.org/10.1161/CIRCHEARTFAILURE.120.00753... |
Journal or Publication Title: | Circulation: Heart Failure |
Volume: | 14 |
Number: | 3 |
Date: | 2021 |
Divisions: | Molecular Cardiology Cardio Genomics |
Depositing User: | General Admin |
Identification Number: | 10.1161/CIRCHEARTFAILURE.120.007537 |
ISSN: | 1941-3289 |
Date Deposited: | 10 Jun 2021 00:59 |
Abstract: | Background: Clinical studies of hypertrophic cardiomyopathy are over-represented by individuals of European ethnicity, with less known about other ethnic groups. We investigated differences between patients in a multiethnic Australian hypertrophic cardiomyopathy population. Methods: We performed a retrospective cohort study of 836 unrelated hypertrophic cardiomyopathy probands attending a specialized clinic between 2002 and 2020. Major ethnic groups were European (n=611), East Asian (n=75), South Asian (n=58), and Middle Eastern and North African (n=68). The minor ethnicity groups were Oceanian (n=9), People of the Americas (n=7), and African (n=8). One-way ANOVA with Dunnett post hoc test and Bonferroni adjustment were performed. Results: Mean age of the major ethnic groups was 54.9±16.9 years, and 527 (65%) were male. Using the European group as the control, East Asian patients had a lower body mass index (29 versus 25 kg/m2, P<0.0001). South Asians had a lower prevalence of atrial fibrillation (10% versus 31%, P=0.024). East Asians were more likely to have apical hypertrophy (23% versus 6%, P<0.0001) and Middle Eastern and North African patients more likely to present with left ventricular outflow tract obstruction (46% versus 34%, P=0.0003). East Asians were less likely to undergo genetic testing (55% versus 85%, P<0.0001) or have an implantable cardioverter-defibrillator implanted (19% versus 36%, P=0.037). East Asians were more likely to have a causative variant in a gene other than MYBPC3 or MYH7, whereas Middle Eastern and North African and South Asians had the highest rates of variants of uncertain significance (27% and 21%, P<0.0001). Conclusions: There are few clinical differences based on ethnicity, but importantly, we identify health disparities relating to access to genetic testing and implantable cardioverter-defibrillator use. Unless addressed, these gaps will likely widen as we move towards precision-medicine-based care of individuals with hypertrophic cardiomyopathy. |
Creators: | Creators Email Butters, Alexandra UNSPECIFIED Semsarian, Caitlin R. UNSPECIFIED Bagnall, Richard D. UNSPECIFIED Yeates, Laura UNSPECIFIED Stafford, Fergus UNSPECIFIED Burns, Charlotte UNSPECIFIED Semsarian, Christopher UNSPECIFIED Ingles, Jodie UNSPECIFIED |
Last Modified: | 10 Jun 2021 00:59 |
URI: | https://eprints.centenary.org.au/id/eprint/1014 |
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